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Assist Clinical Research Manager with the identification and selection of investigators to undertake clinical studies, when required.
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Assist Clinical Research Manager with preparation of study budget.
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Prepare documentation for Ethics Committee submission.
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Coordinate receipt and distribution of clinical trial supplies.
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Prepare and conduct initiation visits.
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Oversee assigned clinical trials to ensure compliance.
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Monitor and document the progress of assigned clinical studies through regular visits and telephone contact with site personnel.
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Liaise with and report to Clinical Research Manager regularly on study status through monitoring reports and meetings.
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Document all study related communications, newsletter etc.
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Perform Source Data Verification to ensure accurate data is recorded.
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Ensure all Serious Adverse Cardiac Events are reported and followed up.
